Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893751
OGG1
0.882 0.240 3 9750423 missense variant G/A;C snv 2.2E-03; 4.0E-06 5
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs104894002
LOC105375056 ; TREM2
0.790 0.320 6 41161557 stop gained G/A snv 2.0E-05 2.1E-05 7
rs1049296
TF
0.882 0.120 3 133775510 missense variant C/T snv 0.16 0.14 4
rs1049564
PNP
0.882 0.160 14 20472447 missense variant G/A snv 0.19 0.21 6
rs10498633
SLC24A4
0.925 0.080 14 92460608 intron variant G/T snv 0.19 2
rs10501320
MADD ; MADD-AS1
0.925 0.120 11 47272248 5 prime UTR variant G/C snv 0.17 5
rs10501602
PICALM
1.000 0.080 11 85970346 intron variant A/G snv 0.10 1
rs1050210428
MAPT
0.925 0.120 17 45983258 missense variant G/A snv 2
rs1050283
OLR1
0.882 0.160 12 10159690 3 prime UTR variant G/A snv 0.40 4
rs1050565
BLMH
1.000 0.080 17 30249058 missense variant T/C snv 0.30 0.29 2
rs10507391
ALOX5AP
0.776 0.320 13 30737959 intron variant A/T snv 0.52 10
rs1051266
SLC19A1
0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs1051338
LIPA
0.807 0.120 10 89247603 missense variant T/G snv 0.32 0.26 7
rs10515639
CAMK2A
1.000 0.080 5 150276863 intron variant C/T snv 0.24 1
rs10516846
SNCA
1.000 0.080 4 89775184 intron variant A/G snv 3.9E-02 1
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs10524523
TOMM40
0.807 0.200 19 44899792 intron variant TTTTTTTTTTTTTTTTTTTTTTT/-;T;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT delins 7
rs1057233
SPI1
1.000 0.080 11 47354897 3 prime UTR variant G/A snv 0.69 1
rs1057518919
PSEN1
0.851 0.120 14 73171023 missense variant T/G snv 5
rs1057519991
TP53
0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 26
rs1057520247
BRCA2
0.882 0.200 13 32326591 synonymous variant C/T snv 7.0E-06 5
rs1060620
LOC112268089 ; GAPDH
1.000 0.080 12 6535556 intron variant A/G;T snv 0.32 1
rs1060743
BIN1
0.925 0.080 2 127068957 synonymous variant A/G snv 0.34 0.29 2
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72